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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1876848Generated: October 26, 2026

p-Toluenesulfonic acid → 1-(isoxazol-5-ylcarbonyl)-4-(4-(2-(4-(1H-pyrazol-1-yl)phenyl)aminopyrimidin-4-yl)-1H-pyrazol-1-yl)piperidin-4-ylacetonitrile

https://huagongshe.com/reaction/1876848

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant4-(1H-Pyrazol-1-yl)anilineHCID 594274—
Reactant(4-(4-(2-chloropyrimidin-4-yl)-1H-pyrazol-1-yl)-1-(isoxazol-5-ylcarbonyl)piperidin-4-yl)acetonitrileHCID 86637284—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Solvent1,4-DioxaneHCID 31275—
Product1-(isoxazol-5-ylcarbonyl)-4-(4-(2-(4-(1H-pyrazol-1-yl)phenyl)aminopyrimidin-4-yl)-1H-pyrazol-1-yl)piperidin-4-ylacetonitrileHCID 58014532—

Reaction Steps

A mixture of (4-(4-(2-chloropyrimidin-4-yl)-1H-pyrazol-1-yl)-1-(isoxazol-5-ylcarbonyl)piperidin-4-yl)acetonitrile (30 mg, 0.08 mmol), 4-(1H-pyrazol-1-yl)aniline (18.9 mg, 0.119 mmol), and p-toluenesulfonic acid (12 mg, 0.067 mmol) in dry 1,4-dioxane (0.6 mL) was refluxed overnight. The mixture was diluted with acetonitrile and water, purified on RP-HPLC to give the desired product as a racemic mixture (22 mg, 52%). LCMS (M+H) 521.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309718B2
Source datasetuspto-grants-2012_11
ORD IDord-f8f71fbfa1804b8a81976b67d7d88f5f
Source noteuspto-grants-2012_11